Anthrax natural history, complications and prognosis: Difference between revisions

Jump to navigation Jump to search
VisualWikitext
m (Changes made per Mahshid's request)
 
(29 intermediate revisions by 2 users not shown)
Line 4: Line 4:


==Overview==
==Overview==
The natural history of anthrax depends on the mode of exposure to the disease (cutaneous, ingestion, inhalation, or injection). In cutaneous anthrax, a small painless [[skin]] sore develops into a [[blister]] and later into a [[skin ulcer]], with a central black area. The resolution of the lesion takes several weeks, depending on its size, location and severity. The anthrax lesions might lead to [[scarring]] and [[contracture]]s. Inhalation anthrax is characterized by a mild initial phase of nonspecific [[symptoms]], that is followed by sudden development of [[dyspnea]], [[cyanosis]], [[disorientation]] with [[coma]], and [[death]].<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref> In oropharyngeal anthrax, the lesion is generally localized in the [[oral cavity]]. This type may progress rapidly, and [[edema]] around the [[lymph node]]s may result in extensive swelling of the neck and anterior [[chest wall]].<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>  The gastrointestinal anthrax lesions may occur anywhere within the [[gastrointestinal tract]], potentially bleeding, and lead to fatal [[hemorrhage]]. Some cases are complicated by massive [[ascites]],[[shock]] and death.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>  The [[prognosis]] of anthrax depends on the form of the disease, how early it is diagnosed, the [[strain]] of [[bacteria]], the patient's age and his health condition. Pulmonary anthrax has the highest [[mortality rate]].<ref name="pmid11851578">{{cite journal| author=Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM et al.| title=Fatal inhalational anthrax in a 94-year-old Connecticut woman. | journal=JAMA | year= 2002 | volume= 287 | issue= 7 | pages= 863-8 | pmid=11851578 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11851578  }} </ref>


==Natural History==
==Natural History==
===Cutaneous Anthrax===
===Cutaneous Anthrax===
The [[incubation period]] of anthrax ranges from as little as 9 hours to 3 weeks, mostly 2 to 6 or 7 days. The natural history of cutaneous anthrax is shown below.     
====Day 0====
====Day 0====
* There is entry of the infecting [[B. anthracis]] (usually as [[spore]]s) through a [[skin]] lesion (cut, abrasion, etc.) or (possibly as vegetative forms or vegetative forms and spores) by means of a fly-bite.
* There is entry of the [[infection|infecting]] [[B. anthracis]] (usually as [[spore]]s) through a [[skin]] lesion (cut, abrasion, etc.) or (possibly as vegetative forms or vegetative forms and spores) by means of a fly-bite.


====Days 2-3====
====Days 2-3====
* A small [[pimple]] or [[papule]] appears.
* A small [[pimple]] or [[papule]] appears.


====Days 3–4====
====Days 3-4====
* A ring of [[vesicle]]s develops around the [[papule]]. Vesicular fluid may be exuded. Unless the patient was treated, capsulated B. anthracis can be identified in appropriately stained smears of this fluid, and the [[bacterium]] can be isolated by culture.
* A ring of [[vesicle]]s develops around the [[papule]]. Vesicular fluid may be exuded. Unless the patient was treated, [[Capsule (microbiology)|capsulated]] [[B. anthracis]] can be identified in appropriately stained smears of this fluid, and the [[bacterium]] can be isolated by [[cell culture|culture]].
* Marked [[edema]] starts to develop.
* Marked [[edema]] starts to develop.
* Unless there is secondary infection, there is no pus and pathognomonically the lesion itself is not painful, although painful [[lymphadenitis]] may occur in the regional [[lymph node]]s and a feeling of pressure may result from the [[edema]].
* Unless there is secondary [[infection]], there is no [[pus]] and pathognomonically the lesion itself is not painful, although painful [[lymphadenitis]] may occur in the regional [[lymph node]]s and a feeling of pressure may result from the [[edema]].
* The lesion is usually 1–3 cm in diameter and remains round and regular. Occasionally a lesion may be larger and irregularly shaped.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* The lesion is usually 1-3 cm in diameter and remains round and regular. Occasionally a lesion may be larger and irregularly shaped.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


====Days 5–7====
====Days 5-7====
* The original [[papule]] ulcerates to form the characteristic [[eschar]]. Topical swabs will not pick up [[B. anthracis]]. Detection in smears or by culture requires lifting the edge of the eschar with tweezers (this gives no pain unless there is secondary infection) and obtaining fluid from underneath. The fluid will probably be sterile if the patient has been treated with an [[antibiotic]].
* The original [[papule]] ulcerates to form the characteristic [[eschar]].
* [[Edema]] extends some distance from the lesion.
* [[Edema]] extends some distance from the lesion.
* Systemic symptoms are [[low-grade fever]], [[malaise]], and [[headache]].
* Systemic [[symptoms]] are [[low-grade fever]], [[malaise]], and [[headache]].
* If the cutaneous reaction is more severe, especially if located on the [[face]], [[neck]], or [[chest]], clinical symptoms may be more severe with more extensive [[edema]] extending from the lesion, toxamia, a change in mental status, high [[fever]], [[hypotension]], regional lymphadenomegaly and the patient unable to eat or drink.
* The [[cutaneous]] reaction is more exacerbated particularly in cases where it is located on the [[face]], [[neck]], or [[chest]]. Clinical [[symptoms]] may be more severe in this case, with extensive [[edema]] around initial lesion, [[toxemia]], change in [[mental status]], high [[fever]], [[hypotension]], regional [[lymphadenopathy|lymphadenomegaly]], affecting the patient's ability to eat or drink.
* [[Tracheotomy]] is a life-saving procedure in patients having a cutaneous lesion on the face or neck with an extensive [[edema]] leading to compression on the [[trachea]]. This clinical manifestation is very dangerous.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* [[Tracheotomy]] is a life-saving procedure in patients who have a [[cutaneous]] lesion on the face or neck, with extensive [[edema]] leading to compression of the [[trachea]]. This clinical manifestation is very dangerous.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


====Day 10====
====Day 10====
* The eschar begins to resolve; resolution takes several weeks and is not hastened by treatment.
* The [[eschar]] begins to resolve; resolution takes several weeks and is not hastened by treatment.
* Clinicians unaware of this suffer from concern that the treatment has been ineffective. A small proportion of untreated cases develop [[sepsis]] or [[meningitis]] with hyperacute symptoms.
* Clinicians unaware of this suffer from concern that the treatment has been ineffective.  
* A small proportion of untreated cases (20%) develop [[sepsis]] or [[meningitis]] with hyperacute [[symptoms]].<ref name="pmid12610093">{{cite journal| author=Spencer RC| title=Bacillus anthracis. | journal=J Clin Pathol | year= 2003 | volume= 56 | issue= 3 | pages= 182-7 | pmid=12610093 | doi= | pmc=PMC1769905 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12610093  }} </ref>


====Time to Resolution====
====Time to Resolution====
* Time to resolution will depend on the size, location and local severity of the lesion.
* Time to resolution will depend on the size, location and local severity of the lesion.
* The initial crust separates several weeks after onset, with subsequent healing by granulation. Sometimes the separation of the crust is delayed and the lesion may become secondarily infected. In this situation, the crust should be excised surgically.
* The initial crust is separated several weeks after the onset, with subsequent healing by granulation. Sometimes the separation of the crust is delayed, and the lesion may become secondarily [[infected]]. In this situation, the crust should be excised surgically.
* Lesions characterized by “malignant edema” can be expected to take months to heal.
* Lesions characterized by “malignant edema” can take months to heal.
* Very large lesions may require skin grafts, and lesions in locations such as the [[eyelid]] may require surgical intervention due to scarring.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* Very large lesions may require [[skin graft]]s, and lesions in locations such as the [[eyelid]] may require surgical intervention due to scarring.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
 
Shown below are images of the development and resolution of uncomplicated cutaneous anthrax lesion.
<gallery>
Image:Cutaneous A1.png| Day 1 of development and resolution of uncomplicated cutaneous anthrax lesion.”<SMALL><SMALL>''[http://www.who.int/en//  Adapted from World Health Organization (WHO)]''<ref name="WHO">{{Cite web | title = World Health Organization | url = http://www.who.int/en/}}</ref></SMALL></SMALL>
 
Image:CutaneousA2.png| Day 2 - 3 of development and resolution of uncomplicated cutaneous anthrax lesion.”<SMALL><SMALL>''[http://www.who.int/en//  Adapted from World Health Organization (WHO)]''<ref name="WHO">{{Cite web | title = World Health Organization | url = http://www.who.int/en/}}</ref></SMALL></SMALL>
 
Image:CutaneousA3.png| Day 4 of development and resolution of uncomplicated cutaneous anthrax lesion.”<SMALL><SMALL>''[http://www.who.int/en//  Adapted from World Health Organization (WHO)]''<ref name="WHO">{{Cite web | title = World Health Organization | url = http://www.who.int/en/}}</ref></SMALL></SMALL>
 
Image:CutaneousA4.png| Day 6 of development and resolution of uncomplicated cutaneous anthrax lesion.”<SMALL><SMALL>''[http://www.who.int/en//  Adapted from World Health Organization (WHO)]''<ref name="WHO">{{Cite web | title = World Health Organization | url = http://www.who.int/en/}}</ref></SMALL></SMALL>
 
Image:CutaneousA5.png| Day 11 of development and resolution of uncomplicated cutaneous anthrax lesion.”<SMALL><SMALL>''[http://www.who.int/en//  Adapted from World Health Organization (WHO)]''<ref name="WHO">{{Cite web | title = World Health Organization | url = http://www.who.int/en/}}</ref></SMALL></SMALL>
</gallery>


===Inhalation Anthrax===
===Inhalation Anthrax===
====Initial Phase====
====Initial Phase====
* Symptoms prior to the onset of the final hyperacute phase are nonspecific, and suspicion of anthrax depends on the knowledge of the patient’s history. The mild initial phase of nonspecific symptoms is followed by the sudden development of [[dyspnea]], [[cyanosis]], [[disorientation]] with [[coma]], and [[death]].  
* [[Symptoms]] prior to the onset of the final hyperacute phase are nonspecific, and suspicion of anthrax depends on the knowledge of the patient’s history. The mild initial phase of nonspecific [[symptoms]] is followed by the sudden development of [[dyspnea]], [[cyanosis]], [[disorientation]] with [[coma]], and [[death]].  


* The typical clinical course of this form of the disease is consistent with the lesion development within the mediastinal [[lymph node]]s before the development of [[bacteraemia]]. The assault on the lung appears to be two-pronged. In the initial phase, the blockade of the lymphatic vessels develops, in association with symptoms such as a sensation of tightness of the chest. Lymphatic stasis is associated with [[edema]], which may be apparent above the thoracic inlet, and [[pleural effusion]]. Histological sections of the lung may reveal [[bacilli]] within the [[lymphatic vessel]]s. In the acute phase, damage associated with [[septicemia]] occurs.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* The typical clinical course of this form of the disease is consistent with the lesion development within the [[mediastinal]] [[lymph node]]s before the development of [[bacteraemia]]. The assault on the lung appears to be two-pronged. In the initial phase, the blockade of the [[lymphatic vessel]]s  develops, in association with [[symptoms]] such as a sensation of tightness of the chest. [[Lymphatic]] [[stasis]] is associated with [[edema]], which may be apparent above the [[thoracic inlet]], and [[pleural effusion]]. [[Histological]] sections of the [[lung]] may reveal [[bacilli]] within the [[lymphatic vessel]]s. In the acute phase, damage associated with [[septicemia]] occurs.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


* Lymphatic stasis resulting from the damaged [[lymph node]]s leads to dilatation of pulmonary lymphatics which originate in the [[pleura]] and drain towards the [[hilum]], following interlobular septa in association with [[blood vessel]]s. The stasis manifests as an early onset [[pleural effusion]] and peripheral infiltrates, representing thickened bronchovascular bundles, detectable on [[chest X-ray]]. These findings mark fully developed initial stage illness.
* [[Lymphatic]] [[stasis]] resulting from the damaged [[lymph node]]s leads to dilatation of [[pulmonary]] lymphatics which originate in the [[pleura]] and drain towards the [[hilum]], following interlobular septa in association with [[blood vessel]]s. The [[stasis]] manifests as an early onset [[pleural effusion]] and peripheral infiltrates, representing thickened bronchovascular bundles, detectable on [[chest X-ray]]. These findings mark fully developed initial stage illness.


====Acute Phase====
====Acute Phase====
* Ultimately, the [[bacteria]] escape from the damaged [[lymph node]]s and invade the blood stream via the thoracic duct. Once the [[bacteremia]] and associated toxemia reach a critical level, the severe symptoms characteristic of the acute phase illness are manifest. During the acute phase illness, damage of the lung tissue becomes apparent on [[X-ray]]. This damage results from the action of anthrax toxin on the [[endothelium]] of the lung’s capillary bed. Primary damage of the [[lung]] is not normally a feature of the initial phase illness and primary pulmonary infection is an uncommon presentation.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* Ultimately, the [[bacteria]] escape from the damaged [[lymph node]]s and invade the [[blood stream]] via the [[thoracic duct]]. Once the [[bacteremia]] and associated [[toxemia]] reach a critical level, the severe [[symptoms]] characteristic of the acute phase illness are manifested. During the acute phase illness, damage of the [[lung]] tissue becomes apparent on the [[X-ray]]. This damage results from the action of anthrax [[toxin]] on the [[endothelium]] of the lung’s capillary bed. Primary damage of the [[lung]] is not normally a feature of the initial phase illness and primary [[pulmonary]] [[infection]] is not common.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


===Ingestion Anthrax===
===Ingestion Anthrax===
====Oropharyngeal anthrax====
====Oropharyngeal anthrax====
* The lesion is generally localized in the oral cavity, especially on the buccal [[mucosa]], [[tongue]], [[tonsil]]s or posterior [[pharynx]] wall. In some cases, lesions may be present at two or more sites along the [[gastrointestinal tract]].
* The lesion is generally localized in the [[oral cavity]], especially on the buccal [[mucosa]], [[tongue]], [[tonsil]]s or posterior [[pharynx]] wall. In some cases, lesions may be present at two or more sites along the [[gastrointestinal tract]].


* The oral lesion is generally 2–3 cm in diameter and covered with a grey pseudomembrane surrounded by extensive [[edema]].
* The [[oral]] lesion is generally 2-3 cm in diameter and covered with a grey pseudomembrane surrounded by extensive [[edema]].


* When the lesion is localized on [[tonsil]]s, the affected [[tonsil]] is also intensely edematous and covered with a grey or white pseudomembrane. [[Tonsil]] lesions may be ulcerated.
* When the lesion is localized on the [[tonsil]]s, the affected [[tonsil]] is also intensely [[edema|edematous]] and covered with a grey or white pseudomembrane. [[Tonsillar]] lesions may be [[ulcer|ulcerated]].


* The main clinical features are [[sore throat]], [[dysphagia]], and painful regional [[lymphadenopathy]] in the involved side of the [[neck]].
* The main clinical features are [[sore throat]], [[dysphagia]], and painful regional [[lymphadenopathy]] in the involved side of the [[neck]].


* The illness may progress rapidly, and [[edema]] around the [[lymph node]] may result in extensive swelling of the neck and anterior [[chest wall]]. The overt infection leads to [[toxemia]], [[acute respiratory distress]] and [[alteration in mental state]]. The patient develops [[acute respiratory distress syndrome]] and may require respiratory support. This clinical picture is followed by [[shock]], [[coma]] and [[death]].
* The illness may progress rapidly, and [[edema]] around the [[lymph node]] may result in extensive swelling of the [[neck]] and anterior [[chest wall]]. The overt [[infection]] leads to [[toxemia]], [[acute respiratory distress]] and [[altered mental status]]. The patient develops [[acute respiratory distress syndrome]] and may require [[respiratory]] support. This clinical picture is followed by [[shock]], [[coma]] and [[death]].


* The lesion and extensive [[edema]] may lead to airway obstruction. In this situation, [[tracheotomy]] is frequently required. Even with treatment, mortality can be high.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* The lesion and extensive [[edema]] may lead to [[airway obstruction]]. In this situation, [[tracheotomy]] is frequently required. Even with treatment, mortality can be high.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


====Gastrointestinal Anthrax====
====Gastrointestinal Anthrax====
* The gastrointestinal anthrax lesion may occur anywhere within the [[gastrointestinal tract]], the [[esophagus]], [[stomach]], [[duodenum]], [[jejunum]], terminal [[ileum]] or [[cecum]], but mostly in the [[ileum]] and [[cecum]].
* The typical [[eschar]] may occur anywhere within the [[gastrointestinal tract]], the [[esophagus]], [[stomach]], [[duodenum]], [[jejunum]], terminal [[ileum]] or [[cecum]], but mostly in the terminal [[ileum]] and [[cecum]].<ref name="pmid12610093">{{cite journal| author=Spencer RC| title=Bacillus anthracis. | journal=J Clin Pathol | year= 2003 | volume= 56 | issue= 3 | pages= 182-7 | pmid=12610093 | doi= | pmc=PMC1769905 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12610093  }} </ref>


*The character of the lesion is generally ulcerative, usually multiple and superficial, surrounded by [[edema]]. These lesions may bleed, [[hemorrhage]] may be massive and fatal, in some cases with [[stomach]] infection. Intestinal lesions may also lead to [[hemorrhage]], obstruction, [[perforation]] or any combination of these. Some cases are complicated with massive [[ascites]] and this leads to [[shock]] and death.
*The character of the lesion is generally [[ulcer|ulcerative]]. There are usually multiple and superficial lesions, surrounded by [[edema]], which may [[bleed]]. [[Hemorrhage]] may be massive and fatal, and in some cases concomitant with [[stomach]] [[infection]]. [[Intestinal]] lesions may also lead to [[hemorrhage]], [[obstruction]], [[perforation]] or any combination of these. Some cases are complicated with massive [[ascites]], potentially leading to [[shock]] and death.


* Pathological examination of intestinal anthrax shows mucosal ulceration with [[edema]], and enlarged and hemorrhagic regional [[lymph node]]s. [[Necrosis]] is sometimes present.
* Pathological examination of intestinal anthrax shows [[mucosal]] [[ulceration]] with [[edema]], and enlarged and [[hemorrhage|hemorrhagic]] regional [[lymph node]]s. [[Necrosis]] is sometimes present.


* The [[infection]] may also be disseminated, and [[sepsis]] with pulmonary or meningeal involvement may result.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>
* The [[infection]] may also be disseminated, and [[sepsis]] with [[pulmonary]] or [[meningeal]] involvement may result.<ref name=WHO>{{cite web | title = Anthrax in Humans and Animals | url = http://www.who.int/csr/resources/publications/anthrax_web.pdf }}</ref>


* The symptoms of gastrointestinal anthrax are initially nonspecific and include:
* The [[symptoms]] of gastrointestinal anthrax may be divided in 2 clinical forms:<ref name="pmid12610093">{{cite journal| author=Spencer RC| title=Bacillus anthracis. | journal=J Clin Pathol | year= 2003 | volume= 56 | issue= 3 | pages= 182-7 | pmid=12610093 | doi= | pmc=PMC1769905 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12610093  }} </ref>
** [[Nausea]]
:* '''Abdominal'''
** [[Vomiting]]
::* [[Asthenia]]
** [[Anorexia]]
::* [[Headache]]
** [[Fainting spells]]
::* [[Nausea]]
** [[Asthenia]]
::* [[Vomiting]]
** Mild [[diarrhea]]
::* [[Anorexia]]
** [[Fever]]
::* [[Fever]]
** [[Headache]]
::* [[Abdominal pain]]
::* [[Bloody diarrhea]]
::* [[Hematemesis]]  
::* [[Fainting spells]]


* In these instances, patients will probably not seek medical treatment and, if they do, intestinal anthrax may not be considered in differential diagnosis. In some cases, approximately 24 hours later the symptoms may become severe and include acute [[diarrhea]], [[nausea]], [[vomiting]], and [[abdominal pain]].
:* '''Oropharyngeal'''
::* [[Fever]]
::* [[Edema]]
::* [[Dysphagia]]
::* [[Sore throat]]
::* Regional [[lymphadenopathy]]


* With progression of the illness, abdominal pain, hematemesis, bloody diarrhea, massive ascites and signs of suggestive acute abdomen (rapid increase in abdominal girth and paroxysms of abdominal pain) appear. Toxemia, sepsis and shock may develop, followed by death.  
* In these instances, patients will probably not seek medical treatment and, if they do, intestinal anthrax may not be considered in [[differential diagnosis]]. In some cases, approximately 24 hours later the [[symptoms]] may become severe and include acute [[diarrhea]], [[nausea]], [[vomiting]], and [[abdominal pain]].  


* The time from onset of symptoms to death has most frequently varied from 2 to 5 days
* With progression of the illness, [[abdominal pain]], [[hematemesis]], [[bloody diarrhea]], massive [[ascites]] and signs of suggestive [[acute abdomen]] (rapid increase in abdominal girth and paroxysms of [[abdominal pain]]) appear. [[Toxemia]], [[sepsis]] and [[shock]] may develop, followed by death.


* The incubation period is typically 1 - 6 days, although it may be as long as 10 days  
* The time between onset of [[symptoms]] to death has frequently varied from 2 to 5 days  


* There is evidence that not all untreated cases end in toxemia, sepsis and death and that, after the initial symptoms, recovery occurs.
* The [[incubation period]] is typically 1 - 6 days, although it may be as long as 10 days
 
* There is evidence that not all untreated cases end in [[toxemia]], [[sepsis]] and death and that, after the initial [[symptoms]], recovery may occur.


==Complications==
==Complications==
===Cutaneous Anthrax===
===Cutaneous and Injection Anthrax===
* Skin lesions may become scarred.  Very large lesions may require skin grafts, and lesions in locations such as the [[eyelid]] may require surgical intervention due to scarring.
* [[Scarring]]
* [[Contracture]]
* [[Meningitis]]
* [[Coma]]


==Gastrointestinal Anthrax===
===Gastrointestinal Anthrax===
* Massive [[ascites]]
* Massive [[ascites]]
* [[Meningitis]]
* [[Shock]]
* [[Shock]]
* [[Coma]]


==Complications==
===Inhalation Anthrax===
* [[Meningitis]]
* [[Shock]]
* [[Coma]]


==Prognosis==
==Prognosis==
The [[anthrax]] [[prognosis]] will depend on a number of factors, including:
* The [[anthrax]] [[prognosis]] depends on a number of factors, including:
*The type of [[anthrax]]
** The type of [[anthrax]]
*How early the [[anthrax]] is diagnosed
** How early the [[anthrax]] is diagnosed
*The [[strain]] of [[anthrax]] [[bacteria]]
** The [[strain]] of [[anthrax]] [[bacteria]]
*The patient's age and health condition
** The patient's age and health condition


Any form of anthrax is treatable if the diagnosis is made early enough and with the appropriate supportive therapy. The pulmonary anthrax is the one with highest mortality rate (45%).<ref name="pmid11851578">{{cite journal| author=Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM et al.| title=Fatal inhalational anthrax in a 94-year-old Connecticut woman. | journal=JAMA | year= 2002 | volume= 287 | issue= 7 | pages= 863-8 | pmid=11851578 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11851578  }} </ref> Mortality rate for other forms is 40%<ref name="pmid14609791">{{cite journal| author=Beatty ME, Ashford DA, Griffin PM, Tauxe RV, Sobel J| title=Gastrointestinal anthrax: review of the literature. | journal=Arch Intern Med | year= 2003 | volume= 163 | issue= 20 | pages= 2527-31 | pmid=14609791 | doi=10.1001/archinte.163.20.2527 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14609791  }} </ref> for the gastrointestinal type, 28%<ref name=NHS>{{cite web | title = An Outbreak of Anthrax Among Drug Users in Scotland, December 2009 to December 2010 | url = http://www.documents.hps.scot.nhs.uk/giz/anthrax-outbreak/anthrax-outbreak-report-2011-12.pdf }}</ref> for the injection type and less than 2% for the cutaneous type.<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_intro }}</ref>
* Any form of anthrax is treatable, if the [[diagnosis]] is made early enough and with the appropriate supportive therapy.


In the non-cutaneneous forms, a correct early diagnosis is harder to reach, so these are associated with particularly high mortality.  
* Following recovery, resolution of small- to medium-size [[cutaneous]] lesions is generally complete with minimal [[scarring]]. With larger lesions, or lesions on mobile areas, scarring and [[contracture]]s may require surgical correction to return normal functioning and large cutaneous defects may require [[skin graft]]ing.


Following recovery, resolution of small- to medium-size cutaneous lesions is generally complete with minimal scarring. With larger lesions, or lesions on mobile areas carring and contractures may require surgical correction to return normal functioning and large cutaneous defects may require skin grafting.
===Mortality===
* In the non-cutaneneous forms, a correct early [[diagnosis]] is harder to reach, so these are associated with particularly high mortality. The pulmonary anthrax is the one with highest mortality rate.<ref name="pmid11851578">{{cite journal| author=Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM et al.| title=Fatal inhalational anthrax in a 94-year-old Connecticut woman. | journal=JAMA | year= 2002 | volume= 287 | issue= 7 | pages= 863-8 | pmid=11851578 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11851578  }} </ref>
 
* The mortality rate for each form of anthrax is:
** Pulmonary anthrax: 45%<ref name="pmid11851578">{{cite journal| author=Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM et al.| title=Fatal inhalational anthrax in a 94-year-old Connecticut woman. | journal=JAMA | year= 2002 | volume= 287 | issue= 7 | pages= 863-8 | pmid=11851578 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11851578  }} </ref>
** Gastrointestinal anthrax: 40%<ref name="pmid14609791">{{cite journal| author=Beatty ME, Ashford DA, Griffin PM, Tauxe RV, Sobel J| title=Gastrointestinal anthrax: review of the literature. | journal=Arch Intern Med | year= 2003 | volume= 163 | issue= 20 | pages= 2527-31 | pmid=14609791 | doi=10.1001/archinte.163.20.2527 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14609791  }} </ref>
** Injection anthrax: 28%<ref name=NHS>{{cite web | title = An Outbreak of Anthrax Among Drug Users in Scotland, December 2009 to December 2010 | url = http://www.documents.hps.scot.nhs.uk/giz/anthrax-outbreak/anthrax-outbreak-report-2011-12.pdf }}</ref>
** Cutaneous anthrax: < 2%<ref name=CDC>{{cite web | title = Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults | url = http://wwwnc.cdc.gov/eid/article/20/2/13-0687_intro }}</ref>


==References==
==References==
{{reflist|2}}
{{reflist|2}}


[[Category:Needs content]]
[[Category:Disease]]
[[Category:Bacterial diseases]]
[[Category:Biological weapons]]
[[Category:Livestock]]
[[Category:Zoonoses]]
[[Category:Medical disasters]]

Latest revision as of 16:38, 18 September 2017

Anthrax Microchapters

Home

Patient Information

Overview

Historical Perspective

Pathophysiology

Causes

Differentiating Anthrax from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Anthrax natural history, complications and prognosis On the Web

Most recent articles

cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Anthrax natural history, complications and prognosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Anthrax natural history, complications and prognosis

CDC on Anthrax natural history, complications and prognosis

Anthrax natural history, complications and prognosis in the news

Blogs on Anthrax natural history, complications and prognosis

Directions to Hospitals Treating Anthrax

Risk calculators and risk factors for Anthrax natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

The natural history of anthrax depends on the mode of exposure to the disease (cutaneous, ingestion, inhalation, or injection). In cutaneous anthrax, a small painless skin sore develops into a blister and later into a skin ulcer, with a central black area. The resolution of the lesion takes several weeks, depending on its size, location and severity. The anthrax lesions might lead to scarring and contractures. Inhalation anthrax is characterized by a mild initial phase of nonspecific symptoms, that is followed by sudden development of dyspnea, cyanosis, disorientation with coma, and death.[1] In oropharyngeal anthrax, the lesion is generally localized in the oral cavity. This type may progress rapidly, and edema around the lymph nodes may result in extensive swelling of the neck and anterior chest wall.[1] The gastrointestinal anthrax lesions may occur anywhere within the gastrointestinal tract, potentially bleeding, and lead to fatal hemorrhage. Some cases are complicated by massive ascites,shock and death.[1] The prognosis of anthrax depends on the form of the disease, how early it is diagnosed, the strain of bacteria, the patient's age and his health condition. Pulmonary anthrax has the highest mortality rate.[2]

Natural History

Cutaneous Anthrax

The incubation period of anthrax ranges from as little as 9 hours to 3 weeks, mostly 2 to 6 or 7 days. The natural history of cutaneous anthrax is shown below.

Day 0

  • There is entry of the infecting B. anthracis (usually as spores) through a skin lesion (cut, abrasion, etc.) or (possibly as vegetative forms or vegetative forms and spores) by means of a fly-bite.

Days 2-3

Days 3-4

  • A ring of vesicles develops around the papule. Vesicular fluid may be exuded. Unless the patient was treated, capsulated B. anthracis can be identified in appropriately stained smears of this fluid, and the bacterium can be isolated by culture.
  • Marked edema starts to develop.
  • Unless there is secondary infection, there is no pus and pathognomonically the lesion itself is not painful, although painful lymphadenitis may occur in the regional lymph nodes and a feeling of pressure may result from the edema.
  • The lesion is usually 1-3 cm in diameter and remains round and regular. Occasionally a lesion may be larger and irregularly shaped.[1]

Days 5-7

Day 10

  • The eschar begins to resolve; resolution takes several weeks and is not hastened by treatment.
  • Clinicians unaware of this suffer from concern that the treatment has been ineffective.
  • A small proportion of untreated cases (20%) develop sepsis or meningitis with hyperacute symptoms.[3]

Time to Resolution

  • Time to resolution will depend on the size, location and local severity of the lesion.
  • The initial crust is separated several weeks after the onset, with subsequent healing by granulation. Sometimes the separation of the crust is delayed, and the lesion may become secondarily infected. In this situation, the crust should be excised surgically.
  • Lesions characterized by “malignant edema” can take months to heal.
  • Very large lesions may require skin grafts, and lesions in locations such as the eyelid may require surgical intervention due to scarring.[1]

Shown below are images of the development and resolution of uncomplicated cutaneous anthrax lesion.

Inhalation Anthrax

Initial Phase

  • Symptoms prior to the onset of the final hyperacute phase are nonspecific, and suspicion of anthrax depends on the knowledge of the patient’s history. The mild initial phase of nonspecific symptoms is followed by the sudden development of dyspnea, cyanosis, disorientation with coma, and death.

Acute Phase

Ingestion Anthrax

Oropharyngeal anthrax

  • The oral lesion is generally 2-3 cm in diameter and covered with a grey pseudomembrane surrounded by extensive edema.

Gastrointestinal Anthrax

  • The symptoms of gastrointestinal anthrax may be divided in 2 clinical forms:[3]
  • Abdominal
  • Oropharyngeal
  • The time between onset of symptoms to death has frequently varied from 2 to 5 days
  • There is evidence that not all untreated cases end in toxemia, sepsis and death and that, after the initial symptoms, recovery may occur.

Complications

Cutaneous and Injection Anthrax

Gastrointestinal Anthrax

Inhalation Anthrax

Prognosis

  • Any form of anthrax is treatable, if the diagnosis is made early enough and with the appropriate supportive therapy.
  • Following recovery, resolution of small- to medium-size cutaneous lesions is generally complete with minimal scarring. With larger lesions, or lesions on mobile areas, scarring and contractures may require surgical correction to return normal functioning and large cutaneous defects may require skin grafting.

Mortality

  • In the non-cutaneneous forms, a correct early diagnosis is harder to reach, so these are associated with particularly high mortality. The pulmonary anthrax is the one with highest mortality rate.[2]
  • The mortality rate for each form of anthrax is:
    • Pulmonary anthrax: 45%[2]
    • Gastrointestinal anthrax: 40%[4]
    • Injection anthrax: 28%[5]
    • Cutaneous anthrax: < 2%[6]

References

  1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 "Anthrax in Humans and Animals" (PDF).
  2. ↑ 2.0 2.1 2.2 Barakat LA, Quentzel HL, Jernigan JA, Kirschke DL, Griffith K, Spear SM; et al. (2002). "Fatal inhalational anthrax in a 94-year-old Connecticut woman". JAMA. 287 (7): 863–8. PMID 11851578.
  3. ↑ 3.0 3.1 3.2 Spencer RC (2003). "Bacillus anthracis". J Clin Pathol. 56 (3): 182–7. PMC 1769905. PMID 12610093.
  4. ↑ Beatty ME, Ashford DA, Griffin PM, Tauxe RV, Sobel J (2003). "Gastrointestinal anthrax: review of the literature". Arch Intern Med. 163 (20): 2527–31. doi:10.1001/archinte.163.20.2527. PMID 14609791.
  5. ↑ "An Outbreak of Anthrax Among Drug Users in Scotland, December 2009 to December 2010" (PDF).
  6. ↑ "Centers for Disease Control and Prevention Expert Panel Meetings on Prevention and Treatment of Anthrax in Adults".
Retrieved from "https://www.wikidoc.org/index.php?title=Anthrax_natural_history,_complications_and_prognosis&oldid=1353665"